search

MeSH 搜索器

Hyperoxaluria, Primary

A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism.
推出的年份: 1991(1987)
副标题
树号: C12.050.351.968.419.313.500, C12.200.777.419.313.500, C12.950.419.313.500, C16.320.565.202.460, C18.452.648.202.460
MeSH 单一 ID: D006960
进入的组:
  • Hyperoxalurias, Primary
  • Primary Hyperoxalurias
  • Primary Hyperoxaluria
  • Primary Oxaluria
  • Oxaluria, Primary
  • Oxalurias, Primary
  • Primary Oxalurias
  • Primary Oxalosis
  • Oxaloses, Primary
  • Oxalosis, Primary
  • Primary Oxaloses

留言 (0)

沒有登入
gif